List of variants in gene RAD21 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_006265.3(RAD21):c.892C>G (p.Pro298Ala)	rs148308569	0.00004
NM_006265.3(RAD21):c.718G>A (p.Gly240Ser)	rs575505257	0.00003
NM_006265.3(RAD21):c.1888A>G (p.Ile630Val)	rs769825200	0.00001
NM_006265.3(RAD21):c.1516C>G (p.Pro506Ala)
NM_006265.3(RAD21):c.193C>G (p.Arg65Gly)	rs1812625715

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